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Sphinganine-1-phosphocholine

group of stereoisomers with the chemical formula C₂₃H₅₁N₂O₅P
ChemicalSubstance group_of_stereoisomers Q105107289
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Sphinganine-1-phosphocholine

Summary

Sphinganine-1-phosphocholine is a group of stereoisomers[1].

Key Facts

  • Sphinganine-1-phosphocholine's instance of is recorded as group of stereoisomers[2].
  • Sphinganine-1-phosphocholine's canonical SMILES is recorded as O=P([O-])(OCCN+(C)C)OCC(N)C(O)CCCCCCCCCCCCCCCN+(C)C)OCC(N)C(O)CCCCCCCCCCCCCCC">[3].
  • Sphinganine-1-phosphocholine's InChI is recorded as InChI=1S/C23H51N2O5P/c1-5-6-7-8-9-10-11-12-13-14-15-16-17-18-23(26)22(24)21-30-31(27,28)29-20-19-25(2,3)4/h22-23,26H,5-21,24H2,1-4H3/t22-,23+/m0/s1[4].
  • Sphinganine-1-phosphocholine's InChIKey is recorded as GSEOJHIBPQRSNH-XZOQPEGZSA-N[5].
  • Sphinganine-1-phosphocholine's chemical formula is recorded as C₂₃H₅₁N₂O₅P[6].
  • Sphinganine-1-phosphocholine's subclass of is recorded as chemical compound[7].
  • Sphinganine-1-phosphocholine's PubChem CID is recorded as 44260122[8].
  • Sphinganine-1-phosphocholine's ChEBI ID is recorded as 132478[9].
  • Sphinganine-1-phosphocholine's found in taxon is recorded as Calanus helgolandicus[10].
  • Sphinganine-1-phosphocholine's isomeric SMILES is recorded as CCCCCCCCCCCCCCCC@@HC@@HCOP(=O)([O-])OCCN+(C)CC@@HC@@HCOP(=O)([O-])OCCN+(C)C">[11].
  • Sphinganine-1-phosphocholine's Human Metabolome Database ID is recorded as HMDB0012082[12].
  • Sphinganine-1-phosphocholine's LIPID MAPS ID is recorded as LMSP01060002[13].
  • Sphinganine-1-phosphocholine's mass is recorded as {'unit': 'http://www.wikidata.org/entity/Q483261', 'amount': '+466.353559362'}[14].
  • Sphinganine-1-phosphocholine's SureChEMBL ID is recorded as 30073142[15].
  • Sphinganine-1-phosphocholine's UniChem compound ID is recorded as 32003901[16].
  • Sphinganine-1-phosphocholine's Probes And Drugs ID is recorded as PD077197[17].

References

Programmatic citations — every numbered marker resolves to a verifiable graph row below.

Direct Wikidata claims

  1. [2] ↑ . wikidata.org.
  2. [3] ↑ . wikidata.org.
  3. [4] ↑ . wikidata.org.
  4. [5] ↑ . wikidata.org.
  5. [6] ↑ . wikidata.org.
  6. [7] ↑ . wikidata.org.
  7. [8] ↑ . PubChem. Retrieved . wikidata.org.
  8. [9] ↑ . ChEBI release 2021-03-01. wikidata.org.
  9. [10] ↑ . The metabolic response of marine copepods to environmental warming and ocean acidification in the absence of food.. wikidata.org.
  10. [11] ↑ . wikidata.org.
  11. [12] ↑ . wikidata.org.
  12. [13] ↑ . LIPID MAPS. Retrieved . lipidmaps.org. Provenance: wikidata.org.
  13. [14] ↑ . wikidata.org.
  14. [15] ↑ . wikidata.org.
  15. [16] ↑ . UniChem. wikidata.org.
  16. [17] ↑ . wikidata.org.

Class ancestry

  1. [1] ↑ . Wikidata. wikidata.org.

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APA 4ort.xyz Knowledge Graph. (2026). Sphinganine-1-phosphocholine. Retrieved May 3, 2026, from https://4ort.xyz/entity/sphinganine-1-phosphocholine
MLA “Sphinganine-1-phosphocholine.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/sphinganine-1-phosphocholine.
BibTeX @misc{4ortxyz_sphinganine-1-phosphocholine_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{Sphinganine-1-phosphocholine}}, year = {2026}, url = {https://4ort.xyz/entity/sphinganine-1-phosphocholine}, note = {Accessed: 2026-05-03}}
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